Variant report

Variant	nsv934076
Chromosome Location	chr6:80656862-80657630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr6:80657155-80657502	H1-hESC	embryonic stem cell:	n/a	chr6:80657435-80657444
2	ATF3	chr6:80657092-80657471	H1-hESC	embryonic stem cell:	n/a	chr6:80657435-80657444
3	BACH1	chr6:80657510-80657774	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr6:80657183-80657755	H1-hESC	embryonic stem cell:	n/a	n/a
5	CREB1	chr6:80657048-80657737	H1-hESC	embryonic stem cell:	n/a	n/a
6	CREB1	chr6:80657124-80657494	A549	lung:	n/a	n/a
7	CREB1	chr6:80657019-80657708	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr6:80656206-80657733	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr6:80657440-80657590	BJ	skin:	n/a	n/a
10	CTCF	chr6:80657300-80657450	GM12866	blood:	n/a	n/a
11	CTCF	chr6:80657232-80657255	MCF-7	breast:	n/a	n/a
12	CTCF	chr6:80656780-80656930	SAEC	small airway:	n/a	chr6:80656836-80656846
13	CTCF	chr6:80657040-80657190	AG04449	skin:	n/a	n/a
14	CTCF	chr6:80657360-80657510	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr6:80656840-80656990	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr6:80656780-80656930	GM12871	blood:	n/a	chr6:80656836-80656846
17	CTCF	chr6:80657186-80657277	NHEK	skin:	n/a	n/a
18	CTCF	chr6:80657140-80657290	HCPEpiC	choroid plexus:	n/a	n/a
19	E2F4	chr6:80657290-80657449	MCF10A-Er-Src	breast:	n/a	chr6:80657429-80657438
20	E2F6	chr6:80657136-80657561	A549	lung:	n/a	chr6:80657279-80657289 chr6:80657153-80657162 chr6:80657151-80657161 chr6:80657429-80657438
21	E2F6	chr6:80656988-80657932	H1-hESC	embryonic stem cell:	n/a	chr6:80657279-80657289 chr6:80657153-80657162 chr6:80657151-80657161 chr6:80657429-80657438
22	E2F6	chr6:80656960-80657622	A549	lung:	n/a	chr6:80657279-80657289 chr6:80657153-80657162 chr6:80657151-80657161 chr6:80657429-80657438
23	E2F6	chr6:80656690-80657999	H1-hESC	embryonic stem cell:	n/a	chr6:80657279-80657289 chr6:80657153-80657162 chr6:80657151-80657161 chr6:80656753-80656762 chr6:80657429-80657438
24	EGR1	chr6:80656989-80657671	MCF-7	breast:	n/a	chr6:80657322-80657336 chr6:80657429-80657438
25	EGR1	chr6:80657014-80657583	H1-hESC	embryonic stem cell:	n/a	chr6:80657322-80657336 chr6:80657429-80657438
26	EGR1	chr6:80657161-80657419	GM12878	blood:	n/a	chr6:80657322-80657336
27	EGR1	chr6:80657193-80657429	K562	blood:	n/a	chr6:80657322-80657336
28	EGR1	chr6:80657000-80657657	ECC-1	luminal epithelium:	n/a	chr6:80657322-80657336 chr6:80657429-80657438
29	EGR1	chr6:80657118-80657399	K562	blood:	n/a	chr6:80657322-80657336
30	EGR1	chr6:80656813-80657622	MCF-7	breast:	n/a	chr6:80657322-80657336 chr6:80657429-80657438
31	EGR1	chr6:80657142-80657571	H1-hESC	embryonic stem cell:	n/a	chr6:80657429-80657438 chr6:80657322-80657336
32	EGR1	chr6:80657217-80657438	GM12878	blood:	n/a	chr6:80657322-80657336 chr6:80657429-80657438
33	EGR1	chr6:80657053-80657595	ECC-1	luminal epithelium:	n/a	chr6:80657322-80657336 chr6:80657429-80657438
34	EP300	chr6:80656445-80657656	SK-N-SH	brain:	n/a	chr6:80656816-80656832 chr6:80657108-80657117 chr6:80656585-80656601 chr6:80657008-80657024 chr6:80656815-80656831 chr6:80657269-80657285 chr6:80656638-80656654 chr6:80656753-80656762
35	FOS	chr6:80657268-80657423	MCF10A-Er-Src	breast:	n/a	n/a
36	FOXP2	chr6:80657077-80657595	SK-N-MC	brain:	n/a	n/a
37	GATA2	chr6:80656129-80657615	SH-SY5Y	brain:	n/a	chr6:80656389-80656400 chr6:80656622-80656629
38	GATA2	chr6:80656102-80656886	HUVEC	blood vessel:	n/a	chr6:80656389-80656400 chr6:80656622-80656629
39	GTF2F1	chr6:80657122-80657717	H1-hESC	embryonic stem cell:	n/a	n/a
40	HA-E2F1	chr6:80656685-80657836	MCF-7	breast:	n/a	chr6:80657279-80657289 chr6:80657153-80657162 chr6:80657151-80657161 chr6:80656753-80656762 chr6:80657429-80657438
41	HDAC2	chr6:80657364-80657802	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUN	chr6:80657416-80657471	H1-hESC	embryonic stem cell:	n/a	n/a
43	JUND	chr6:80657035-80657766	H1-hESC	embryonic stem cell:	n/a	n/a
44	KAP1	chr6:80655822-80657185	HEK293	kidney:	n/a	n/a
45	KAP1	chr6:80657389-80657991	HEK293	kidney:	n/a	n/a
46	MAX	chr6:80656842-80657910	H1-hESC	embryonic stem cell:	n/a	n/a
47	MAX	chr6:80656974-80657702	A549	lung:	n/a	n/a
48	MAX	chr6:80657062-80657589	HepG2	liver:	n/a	n/a
49	MAX	chr6:80656935-80657974	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAX	chr6:80656422-80657701	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:80657412-80657462	HRPEpiC	eye:	n/a
2	chr6:80656973-80657023	BE2_C	brain:	n/a
3	chr6:80657412-80657462	HRPEpiC	eye:	n/a
4	chr6:80656973-80657023	BE2_C	brain:	n/a
5	chr6:80657555-80657605	Caco-2	colon:	n/a
6	chr6:80657193-80657243	SK-N-SH	brain:	n/a
7	chr6:80657542-80657592	Hela-S3	cervix:	n/a
8	chr6:80656888-80656938	GM12891	blood:	n/a
9	chr6:80657555-80657605	SK-N-SH_RA	brain:	n/a
10	chr6:80657436-80657486	AoSMC	blood vessel:	n/a
11	chr6:80657415-80657465	HNPCEpiC	eye:	n/a
12	chr6:80657412-80657462	HNPCEpiC	eye:	n/a
13	chr6:80656888-80656938	BJ	skin:	n/a
14	chr6:80657542-80657592	HL-60	blood:	n/a
15	chr6:80657415-80657465	PFSK-1	brain:	n/a
16	chr6:80657542-80657592	PrEC	prostate:	n/a
17	chr6:80657555-80657605	PFSK-1	brain:	n/a
18	chr6:80657412-80657462	HL-60	blood:	n/a
19	chr6:80657193-80657243	SAEC	small airway:	n/a
20	chr6:80657412-80657462	MCF10A-Er-Src	breast:	n/a
21	chr6:80657555-80657605	HEEpiC	esophagus:	n/a
22	chr6:80657193-80657243	HUVEC	blood vessel:	n/a
23	chr6:80657542-80657592	AG10803	skin:	n/a
24	chr6:80656888-80656938	HNPCEpiC	eye:	n/a
25	chr6:80657428-80657478	RPTEC	kidney:	n/a
26	chr6:80657436-80657486	SKMC	muscle:	n/a
27	chr6:80656973-80657023	GM06990	blood:	n/a
28	chr6:80657193-80657243	HCM	heart:	n/a
29	chr6:80657412-80657462	Hela-S3	cervix:	n/a
30	chr6:80657412-80657462	Caco-2	colon:	n/a
31	chr6:80656973-80657023	AG04449	skin:	fetal
32	chr6:80657430-80657480	BE2_C	brain:	n/a
33	chr6:80656973-80657023	AG10803	skin:	n/a
34	chr6:80657428-80657478	AG10803	skin:	n/a
35	chr6:80657415-80657465	BJ	skin:	n/a
36	chr6:80657412-80657462	MCF-7	breast:	n/a
37	chr6:80656973-80657023	Jurkat	blood:	n/a
38	chr6:80657193-80657243	BE2_C	brain:	n/a
39	chr6:80657412-80657462	HIPEpiC	eye:	n/a
40	chr6:80657415-80657465	Hepatocyte	liver:	n/a
41	chr6:80657436-80657486	HCM	heart:	n/a
42	chr6:80657430-80657480	AG10803	skin:	n/a
43	chr6:80657193-80657243	GM12892	blood:	n/a
44	chr6:80657430-80657480	MCF10A-Er-Src	breast:	n/a
45	chr6:80657430-80657480	HAEpiC	amniotic membrane:	n/a
46	chr6:80656888-80656938	AoSMC	blood vessel:	n/a
47	chr6:80657555-80657605	RPTEC	kidney:	n/a
48	chr6:80657542-80657592	H1-hESC	embryonic stem cell:	embryo
49	chr6:80657430-80657480	GM12892	blood:	n/a
50	chr6:80657555-80657605	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:80656144..80658220-chr6:80712686..80714230,2	K562	blood:
2	chr1:149858428..149860800-chr6:80655814..80658112,2	MCF-7	breast:
3	chr6:80654201..80657156-chr6:80707214..80709323,2	MCF-7	breast:

Variant related genes	Relation type
ELOVL4	TF binding region
ELOVL4	CpG island
ENSG00000184260	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000112742	chromatin interactions

Extended variants
information (count: 32 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538170829	chr6:80656867-80656868	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs555103383	chr6:80656874-80656875	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs575090957	chr6:80656917-80656918	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs377160316	chr6:80656942-80656943	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs540728291	chr6:80656976-80656977	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs370640128	chr6:80657003-80657004	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs373355245	chr6:80657011-80657012	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs202106960	chr6:80657033-80657034	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs577297974	chr6:80657077-80657078	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs62407622	chr6:80657086-80657087	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs562763990	chr6:80657094-80657095	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs530801492	chr6:80657099-80657100	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs374986643	chr6:80657159-80657160	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs370635051	chr6:80657223-80657224	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs240307	chr6:80657232-80657233	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs376652433	chr6:80657241-80657242	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs560742982	chr6:80657245-80657246	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs539142746	chr6:80657248-80657249	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs200403099	chr6:80657255-80657256	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs546271509	chr6:80657264-80657265	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs566258062	chr6:80657276-80657277	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs559131282	chr6:80657288-80657289	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs538376275	chr6:80657307-80657308	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs374411961	chr6:80657332-80657333	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs552115192	chr6:80657348-80657349	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs75912037	chr6:80657423-80657424	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs538486068	chr6:80657428-80657429	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs555010506	chr6:80657446-80657447	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs376515971	chr6:80657457-80657458	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs575077004	chr6:80657507-80657508	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs111607692	chr6:80657526-80657527	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs554289359	chr6:80657568-80657569	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80654400-80657600	Active TSS	Brain Anterior Caudate	brain
2	chr6:80654600-80657400	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr6:80654800-80657800	Active TSS	Brain Angular Gyrus	brain
4	chr6:80655600-80657400	Active TSS	Right Atrium	heart
5	chr6:80655600-80657400	Active TSS	NHDF-Ad	bronchial
6	chr6:80655600-80657600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:80655600-80659400	Active TSS	Thymus	Thymus
8	chr6:80655800-80657400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:80655800-80657400	Active TSS	NHLF	lung
10	chr6:80655800-80657600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:80655800-80657600	Active TSS	Brain Hippocampus Middle	brain
12	chr6:80655800-80657600	Active TSS	Fetal Brain Male	brain
13	chr6:80655800-80657800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:80655800-80657800	Active TSS	Stomach Smooth Muscle	stomach
15	chr6:80655800-80658000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr6:80656000-80657000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr6:80656000-80657000	Flanking Active TSS	HUVEC	blood vessel
18	chr6:80656000-80657400	Active TSS	H1 Cell Line	embryonic stem cell
19	chr6:80656000-80657400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:80656000-80657400	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr6:80656000-80657400	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr6:80656000-80657400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:80656000-80657400	Active TSS	Brain Cingulate Gyrus	brain
24	chr6:80656000-80657400	Active TSS	Dnd41	blood
25	chr6:80656000-80657600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:80656000-80657600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:80656000-80657600	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr6:80656000-80657600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr6:80656000-80657600	Active TSS	HSMM	muscle
30	chr6:80656000-80657800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr6:80656000-80657800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:80656000-80657800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr6:80656000-80657800	Active TSS	Aorta	Aorta
34	chr6:80656000-80657800	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr6:80656000-80658000	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr6:80656200-80657000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr6:80656200-80657000	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
38	chr6:80656200-80657000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
39	chr6:80656200-80657000	Active TSS	Fetal Heart	heart
40	chr6:80656200-80657000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
41	chr6:80656200-80657200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
42	chr6:80656200-80657400	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr6:80656200-80657400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr6:80656200-80657400	Bivalent/Poised TSS	Fetal Intestine Large	intestine
45	chr6:80656200-80657400	Active TSS	Rectal Smooth Muscle	rectum
46	chr6:80656200-80657400	Active TSS	HMEC	breast
47	chr6:80656200-80657400	Active TSS	HSMMtube	muscle
48	chr6:80656200-80657600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:80656200-80657600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:80656200-80657600	Active TSS	H9 Cell Line	embryonic stem cell

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